[go: up one dir, main page]

PE20121732A1 - SPIRO-CONDENSED CYCLOHEXANE DERIVATIVES AS USEFUL INHIBITORS OF HSL IN THE TREATMENT OF DIABETES - Google Patents

SPIRO-CONDENSED CYCLOHEXANE DERIVATIVES AS USEFUL INHIBITORS OF HSL IN THE TREATMENT OF DIABETES

Info

Publication number
PE20121732A1
PE20121732A1 PE2012000489A PE2012000489A PE20121732A1 PE 20121732 A1 PE20121732 A1 PE 20121732A1 PE 2012000489 A PE2012000489 A PE 2012000489A PE 2012000489 A PE2012000489 A PE 2012000489A PE 20121732 A1 PE20121732 A1 PE 20121732A1
Authority
PE
Peru
Prior art keywords
phenyl
hsl
spiro
diabetes
treatment
Prior art date
Application number
PE2012000489A
Other languages
Spanish (es)
Inventor
Jean Ackermann
Stephan Brugger
Aurelia Conte
Daniel Huziker
Werner Neidhart
Matthias Nettekoven
Tanja Schulz-Gasch
Stanley Wertheimer
Original Assignee
Hoffmann La Roche
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of PE20121732A1 publication Critical patent/PE20121732A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/54Spiro-condensed
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/06Antihyperlipidemics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/12Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Diabetes (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Cardiology (AREA)
  • Epidemiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pain & Pain Management (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Child & Adolescent Psychology (AREA)
  • Emergency Medicine (AREA)
  • Rheumatology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Endocrinology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

SE REFIERE A COMPUESTOS DERIVADOS DE CICLOHEXANO ESPIRO-CONDENSADO DE FORMULA (I) DONDE R1 ES ALQUILO, FENILO, FENILALQUILO, PIRIDINILO, PIRAZOLILO, ENTRE OTROS; R2 ES H, ALQUILO, CICLOALQUILO, OXETANILALCOXILALQUILO, HIDROXIALQUILO, ENTRE OTROS; R3 ES R4-A- O ESTA AUSENTE SI Ca Y Cb SE UNEN POR UN DOBLE ENLACE, EN DONDE R4 ES H, ALQUILO, CICLOALQUILO, FENILO, ENTRE OTROS; A ES O, S, S(O), S(O)2, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: (5a,8b)-8-HIDROXI-2-(4-TRIFLUOROMETOXI-FENIL)-2-AZA-ESPIRO[4.5]DECAN-1-ONA; (5a,8b)-2-(4-ETIL-FENIL)-1-OXO-2-AZA-ESPIRO[4.5]DEC-8-IL] ESTER DEL ACIDO (3-FLUORO-BENCIL)-CARBAMICO; (5a,8b)-8-HIDROXI-8-ISOPROPIL-2-[4-(2,2,2-TRIFLUORO-ETOXI)-FENIL]-2-AZA-ESPIRO[4.5]DECAN-1-ONA; ENTRE OTROS. TAMBIEN SE REFIERE A UN PROCEDIMIENTO DE PREPARACION Y UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA LIPASA SENSIBLE A HORMONAS (HSL) SIENDO UTILES EN EL TRATAMIENTO DE DIABETES, SINDROME METABOLICO, OBESIDADREFERS TO COMPOUNDS DERIVED FROM SPIRO-CONDENSED CYCLOHEXANE OF FORMULA (I) WHERE R1 IS ALKYL, PHENYL, PHENYLALKYL, PYRIDINYL, PIRAZOLIL, AMONG OTHERS; R2 IS H, ALKYL, CYCLOALKYL, OXETANYLALCOXYLALKYL, HYDROXYALKYL, AMONG OTHERS; R3 IS R4-A- OR IS ABSENT IF Ca AND Cb ARE JOINED BY A DOUBLE LINK, WHERE R4 IS H, ALKYL, CYCLOALKYL, PHENYL, AMONG OTHERS; A IS O, S, S (O), S (O) 2, AMONG OTHERS. PREFERRED COMPOUNDS ARE: (5a, 8b) -8-HYDROXY-2- (4-TRIFLUOROMETOXY-PHENYL) -2-AZA-SPYRO [4.5] DECAN-1-ONA; (5a, 8b) -2- (4-ETHYL-PHENYL) -1-OXO-2-AZA-SPYRO [4.5] DEC-8-IL] (3-FLUORO-BENZYL) -CARBAMIC ACID ESTER; (5a, 8b) -8-HYDROXY-8-ISOPROPYL-2- [4- (2,2,2-TRIFLUORO-ETOXY) -PHENYL] -2-AZA-SPYRO [4.5] DECAN-1-ONA; AMONG OTHERS. IT ALSO REFERS TO A PREPARATION PROCEDURE AND A PHARMACEUTICAL COMPOSITION. SAID COMPOUNDS ARE INHIBITORS OF HORMONE SENSITIVE LIPASE (HSL), BEING USEFUL IN THE TREATMENT OF DIABETES, METABOLIC SYNDROME, OBESITY

PE2012000489A 2009-10-15 2010-10-12 SPIRO-CONDENSED CYCLOHEXANE DERIVATIVES AS USEFUL INHIBITORS OF HSL IN THE TREATMENT OF DIABETES PE20121732A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP09173178 2009-10-15

Publications (1)

Publication Number Publication Date
PE20121732A1 true PE20121732A1 (en) 2012-12-28

Family

ID=43093680

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2012000489A PE20121732A1 (en) 2009-10-15 2010-10-12 SPIRO-CONDENSED CYCLOHEXANE DERIVATIVES AS USEFUL INHIBITORS OF HSL IN THE TREATMENT OF DIABETES

Country Status (20)

Country Link
US (1) US8440710B2 (en)
EP (1) EP2488493B1 (en)
JP (1) JP5749272B2 (en)
KR (1) KR101576328B1 (en)
CN (1) CN102858743B (en)
AR (1) AR078619A1 (en)
AU (1) AU2010305859A1 (en)
BR (1) BR112012008962A2 (en)
CA (1) CA2776457A1 (en)
CL (1) CL2012000937A1 (en)
ES (1) ES2538005T3 (en)
IL (1) IL218958A0 (en)
IN (1) IN2012DN03337A (en)
MX (1) MX2012004311A (en)
PE (1) PE20121732A1 (en)
PH (1) PH12012500630A1 (en)
RU (1) RU2607080C2 (en)
TW (1) TW201118068A (en)
WO (1) WO2011045292A1 (en)
ZA (1) ZA201202613B (en)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SI2411395T1 (en) 2009-03-23 2013-07-31 Glenmark Pharmaceuticals S.A. Furopyrimidinedione derivatives as trpa1 modulators
US8097634B2 (en) * 2010-04-15 2012-01-17 Hoffmann-La Roche Inc. Azacyclic derivatives
US8722721B2 (en) * 2011-03-16 2014-05-13 Hoffmann-La Roche Inc. SEC-hydroxycyclohexyl derivatives
US8703807B2 (en) * 2011-03-17 2014-04-22 Hoffmann-La Roche Inc. Azaspirodecanone compounds
US8809384B2 (en) 2011-03-25 2014-08-19 Hoffmann-La Roche Inc. Azaspirodecanone compounds
CN103319395B (en) * 2013-04-08 2014-09-24 武汉罗化科技有限公司 A kind of industrial preparation method and product of 4-fluoroisatin
WO2015103756A1 (en) * 2014-01-09 2015-07-16 Merck Sharp & Dohme Corp. Inhibitors of the renal outer medullary potassium channel
UY36060A (en) 2014-04-02 2015-10-30 Bayer Pharma AG AZOL COMPOUNDS REPLACED WITH AMIDA
KR102732404B1 (en) 2017-11-01 2024-11-19 브리스톨-마이어스 스큅 컴퍼니 Alkene compounds as farnesoid X receptor modulators
KR102732405B1 (en) 2017-11-01 2024-11-20 브리스톨-마이어스 스큅 컴퍼니 Alkene spirocyclic compounds as farnesoid X receptor modulators
CA3081424A1 (en) 2017-11-01 2019-05-09 Bristol-Myers Squibb Company Spirocyclic compounds as farnesoid x receptor modulators
AR113820A1 (en) 2017-11-01 2020-06-17 Bristol Myers Squibb Co BRIDGE BICYCLIC COMPOUNDS AS MODULATORS OF THE X FARNESOID RECEIVER
WO2019089664A1 (en) 2017-11-01 2019-05-09 Bristol-Myers Squibb Company Multicyclic compounds as farnesoid x receptor modulators
CN109369354B (en) * 2018-12-15 2021-07-09 浦拉司科技(上海)有限责任公司 A kind of synthetic method of 4,4,4-trifluorobutanol
SG11202108794RA (en) 2019-02-15 2021-09-29 Bristol Myers Squibb Co Substituted amide compounds useful as farnesoid x receptor modulators
KR102883856B1 (en) 2019-02-15 2025-11-10 브리스톨-마이어스 스큅 컴퍼니 Substituted amide compounds useful as farnesoid X receptor modulators
AR118050A1 (en) 2019-02-15 2021-09-15 Bristol Myers Squibb Co BICYCLIC COMPOUNDS REPLACED AS MODULATORS OF THE FARNESOID X RECEIVER
EP3924337A1 (en) 2019-02-15 2021-12-22 Bristol-Myers Squibb Company Substituted bicyclic compounds as farnesoid x receptor modulators
CN117567380B (en) * 2023-11-17 2025-10-17 广东药科大学附属第一医院 Triazole HSL inhibitor, preparation method and application thereof

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10247680B4 (en) * 2002-10-12 2005-09-01 Aventis Pharma Deutschland Gmbh New bicyclic inhibitors of the hormone sensitive lipase
US7320992B2 (en) 2003-08-25 2008-01-22 Amgen Inc. Substituted 2,3-dihydro-1h-isoindol-1-one derivatives and methods of use
CA2549510A1 (en) 2003-12-16 2005-07-07 Pfizer Products Inc. Pyrido[2,3-d]pyrimidine-2,4-diamines as pde 2 inhibitors
FR2870538B1 (en) * 2004-05-19 2006-07-14 Servier Lab NOVEL DERIVATIVES OF PYRROLIDINES AND THIAZOLIDINES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
US20070208001A1 (en) 2006-03-03 2007-09-06 Jincong Zhuo Modulators of 11- beta hydroxyl steroid dehydrogenase type 1, pharmaceutical compositions thereof, and methods of using the same
PL2021337T3 (en) * 2006-04-25 2010-06-30 Lilly Co Eli Inhibitors of 11-beta-hydroxysteroid dehydrogenase 1
AU2007244861B2 (en) 2006-04-25 2012-03-15 Eli Lilly And Company Inhibitors of 11-beta-hydroxysteroid dehydrogenase 1
GB0705656D0 (en) 2007-03-23 2007-05-02 Addex Pharmaceuticals Sa Novel compounds E1

Also Published As

Publication number Publication date
PH12012500630A1 (en) 2012-10-22
HK1179957A1 (en) 2013-10-11
KR20120074304A (en) 2012-07-05
CL2012000937A1 (en) 2012-09-14
US8440710B2 (en) 2013-05-14
CN102858743A (en) 2013-01-02
CN102858743B (en) 2015-06-10
US20110092512A1 (en) 2011-04-21
RU2012119706A (en) 2013-11-20
BR112012008962A2 (en) 2019-09-24
ZA201202613B (en) 2013-01-30
CA2776457A1 (en) 2011-04-21
KR101576328B1 (en) 2015-12-10
AR078619A1 (en) 2011-11-23
EP2488493A1 (en) 2012-08-22
MX2012004311A (en) 2012-04-30
RU2607080C2 (en) 2017-01-10
JP2013507421A (en) 2013-03-04
ES2538005T3 (en) 2015-06-16
IN2012DN03337A (en) 2015-10-23
EP2488493B1 (en) 2015-04-15
WO2011045292A1 (en) 2011-04-21
TW201118068A (en) 2011-06-01
JP5749272B2 (en) 2015-07-15
AU2010305859A1 (en) 2012-06-07
IL218958A0 (en) 2012-06-28

Similar Documents

Publication Publication Date Title
PE20121732A1 (en) SPIRO-CONDENSED CYCLOHEXANE DERIVATIVES AS USEFUL INHIBITORS OF HSL IN THE TREATMENT OF DIABETES
UY29575A1 (en) POLYMODIC FORMS OF ETHYL ETHYL ESTER 3 - ((2 - ((4- (HEXILOXICARBONILAMINO - IMINO-METIL) -PENYLAMINO) -METIL) -1-METHYL-BENCIMIDAZOL-5-CARBONIL) -PIRIDIN-2-IL - -AMINO) -PROPIÓNICO
PE20110136A1 (en) ORGANIC COMPOUNDS
PE20091002A1 (en) DIPEPTIDED ANALOGS AS INHIBITORS OF THE COAGULATION FACTOR
UY28493A1 (en) METHYLOSULPHONATE OF ETHYL ETHYL ESTER 3 - ((2 - ((4- (HEXILOXICARBONILAMINO-IMINO-METTIL) -PENYLAMINO) -METIL) -1-METHYL-1H-BENCIMIDAZOL-5-CARBONIL) -PIRIDIN-2-IL-AMINO ) -PROPIONIC AND ITS USE AS A MEDICINAL PRODUCT.
CL2008000422A1 (en) The compound 4- [4- (2-adamantylcarbamoyl) -5-tert-butylpyrazol-1-yl] -benzoic acid; pharmaceutical composition; its use as an inhibitor of 11bhsd1, useful in the treatment of type 2 diabetes and obesity.
PE20142019A1 (en) NEW DERIVATIVES OF INDANYLOXIDIHIDROBENZOFURANILACETICOS ACIDS AND THEIR USES AS AGONISTS OF THE GPR40 RECEPTOR
NZ601121A (en) 5-alkynyl-pyrimidines
NZ716420A (en) Fused heterocyclic compounds as sodium channel modulators
PE20141682A1 (en) (4-PHENYLIMIDAZOLE-2-IL) ETHYLAMINE DERIVATIVES USEFUL AS SODIUM CHANNEL MODULATORS
PE20120690A1 (en) DERIVATIVES OF 5-FLUOROPYRIMIDINONE
NO20091548L (en) Imidazolone and imidazolidinone derivatives as 11B-HSD1 inhibitors of diabetes
TN2012000125A1 (en) Substituted carbamoylmethylamino acetic acid derivatives as novel nep inhibitors
EA201101671A1 (en) SUBSTITUTED DERIVATIVES OF AMINOPROPIONIC ACID AS NEPRILISIN INHIBITORS
EA201390198A1 (en) Heterocyclic Compound
PE20090547A1 (en) PIRAZINONE DERIVATIVES AS p38 KINASE INHIBITORS
PE20091828A1 (en) CONDENSED CYCLOPENTANOCARBOXYLIC ACID DERIVATIVES REPLACED WITH ACILAMINE AS EDG-2 INHIBITORS
PE20120585A1 (en) CRYSTALLINE FORM OF DIHYDROGEN PHOSPHATE R) -3- (4- (2- (2-METHYLTETRAZOLE-5-IL) PYRIDIN-5-IL) -3-FLUOROFENSIL) -5-HYDROXIMETHYL OXAZOLIDIN-2-ONA
MX339252B (en) Pyrrolidine or thiazolidine carboxylic acid derivatives, pharmaceutical composition and methods for use in treating metabolic disordersas as agonists of g- protein coupled receptor 43 (gpr43).
MX2010008583A (en) Novel crystalline forms of 4- [4- (2-adamantylcarbam0yl) -5-tert-butyl-pyrazol-1-yl] benzoic acid.
WO2012161518A3 (en) Novel thiourea derivatives as activators of rorα and pharmaceutical composition containing same
MX2011012199A (en) Benzoxazolone derivatives as aldosterone symthase inhibitors.
EA201390643A1 (en) CRYSTAL FORMS OF HYDROCHLORIDE (4A-R, 9A-S) -1- (1H-BENZOIMIDAZOLE-5-CARBONYL-2,3,4,4A, 9,9A-HEXAHYDRO-1H-INDENO [2,1-B] PYRIDIN- 6-CARBONITRILE AND THEIR APPLICATION AS HSD 1 INHIBITORS
ECSP11010849A (en) N- (2-AMINOPHENYL) -4- [N- (PIRIDIN-3-IL) METOXICARBONYLAMINE-METHYL] POLYMORPH B BENZAMIDE (MS-275)
WO2011047055A3 (en) Novel mek inhibitors, useful in the treatment of diseases

Legal Events

Date Code Title Description
FA Abandonment or withdrawal